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Thalidomide and Congenital Abnormalities - Thornlea

Thalidomide and Congenital Abnormalities - Thornlea

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THALIDOMIDE AND CONGENITAL ABNORMALITIESThe Lancet, to alert the medical community to thedangers of thalidomide.nPRIMARY SOURCETHALIDOMIDE AND CONGENITAL ABNORMALITIESSIR,—<strong>Congenital</strong> abnormalities are present in approximately15% of babies. In recent months I have observedthat the incidence of multiple severe abnormalities inbabies delivered of women who were given the drug thalidomide(‘Distaval’) during pregnancy, as an anti-emetic oras a sedative, to be almost 20%.These abnormalities are present in structures developedfrom mesenchyme—i.e., the bones <strong>and</strong> musculatureof the gut. Bony development seems to be affected in avery striking manner, resulting in polydactyly, syndactyly,<strong>and</strong> failure of development of long bones (abnormally shortfemora <strong>and</strong> radii).Have any of your readers seen similar abnormalities inbabies delivered of women who have taken this drug duringpregnancy?Hurstville, New South Wales.W. G. MCBRIDE.nnnA young thalidomide victim, born without arms, clutches abouquet with her toes as she presents it to Princess Anne ofGreat Britain in 1972. ªBETTMANN/CORBIS.SIGNIFICANCEMcBride’s warning concerning the teratogeniceffects of thalidomide saved countless babies frombeing born with birth defects. However, the drugremained on the market for some time followingMcBride’s warning, which accounts for the fact thatthere are still some 8,000 thalidomide survivors in theworld today.The observations of McBride <strong>and</strong> Lenz were tohave far-reaching effects on the pharmaceutical industry.They were astute enough to notice rare <strong>and</strong> unusualconditions occurring in their patients <strong>and</strong> to spotpatterns <strong>and</strong> connections with factors such as drugexposure. After thalidomide, it became m<strong>and</strong>atory totest new drugs on pregnant animals. Doctors becamefar more aware of the potential teratogenic effect ofdrugs <strong>and</strong> were more careful about the drugs theyprescribed to pregnant women.In general, the drug regulatory authoritiesacquired more sweeping powers after the thalidomidetragedy. One important development was the establishmentof systems for post-market drug surveillance.That is, once a drug is on the market, it is monitoredfor any new side effects that emerge in the generalpopulation. These new side effects are reportedthrough the physician. As a result of these postmarketingsurveillance efforts, several drugs havebeen withdrawn on safety grounds. Unanticipateddrug side effects still occur <strong>and</strong> they still harm oreven kill vulnerable people. However, tighter regulationhas undoubtedly improved patient safety.Meanwhile, thalidomide has enjoyed somethingof a resurgence as a treatment for leprosy <strong>and</strong> multiplemyeloma. However, it is no longer prescribed towomen who are pregnant or who may become pregnant.Scientists now know that other drugs are asdangerous to an unborn child as thalidomide is. Onesuch drug is isotretinoin, which is used in the treatmentof severe acne. A woman actually needs to provideproof of a negative pregnancy test before she canbe prescribed isotretinoin, according to the U.S.Food <strong>and</strong> Drug Administration. While on the drug,she must use an effective method of contraception.The fetus is most vulnerable to medication exposurethrough the placenta in the first three months ofpregnancy. In the thalidomide case, one in fivewomen who had taken the drug between thirtyseven<strong>and</strong> fifty-four days of pregnancy gave birth toa child with birth defects.292 MEDICINE, HEALTH, AND BIOETHICS: ESSENTIAL PRIMARY SOURCES

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